日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

The BCL2 family: from apoptosis mechanisms to new advances in targeted therapy

BCL2家族:从细胞凋亡机制到靶向治疗的新进展

Vogler, Meike; Braun, Yannick; Smith, Victoria M; Westhoff, Mike-Andrew; Pereira, Raquel S; Pieper, Nadja M; Anders, Marius; Callens, Manon; Vervliet, Tim; Abbas, Maha; Macip, Salvador; Schmid, Ralf; Bultynck, Geert; Dyer, Martin Js

Disturbed Spatial WNT Activation-A Potential Driver of the Reticularized Skin Phenotype in Systemic Sclerosis.

空间 WNT 激活紊乱——系统性硬化症网状皮肤表型的潜在驱动因素

Fakhouri Sara Chenguiti, Zhu Honglin, Li Yi-Nan, Ronicke Moritz, Rigau Aleix Rius, Dees Clara, Konstantinidis Laura, Schmid Ralf, Matei Alexandru-Emil, Eckstein Markus, Geppert Carol, Ludolph Ingo, Kreuter Alexander, Sticherling Michael, Berking Carola, Horch Raymund E, Schett Georg, Distler Jörg H W, Bergmann Christina

BTK mutations in patients with chronic lymphocytic leukemia receiving tirabrutinib

接受替拉布替尼治疗的慢性淋巴细胞白血病患者的BTK突变

Jackson, Ross A; Britton, Robert G; Jayne, Sandrine; Lehmann, Susann; Cowley, Caroline M; Trethewey, Christopher S; Smith, Victoria M; Schmid, Ralf; Fegan, Christopher; Walter, Harriet S; Dyer, Martin J S

Limitations of Monitoring Disease Progression Using Circulating Tumor DNA in Lymphoma: An Example From Primary Cutaneous DLBCL Leg-type

利用循环肿瘤DNA监测淋巴瘤疾病进展的局限性:以原发性皮肤弥漫性大B细胞淋巴瘤腿型为例

Trethewey, Christopher S; Walter, Harriet S; Alqahtani, Abdullah N M; Schmid, Ralf; Guttery, David S; Griffin, Yvette; Ahearne, Matthew J; Saldanha, Gerald S; Jayne, Sandrine P N; Dyer, Martin J S

Correction: Discovery of a heme-binding domain in a neuronal voltage-gated potassium channel

更正:在神经元电压门控钾通道中发现血红素结合域

Burton, Mark J; Cresser-Brown, Joel; Thomas, Morgan; Portolano, Nicola; Basran, Jaswir; Freeman, Samuel L; Kwon, Hanna; Bottrill, Andrew R; Llansola-Portoles, Manuel J; Pascal, Andrew A; Jukes-Jones, Rebekah; Chernova, Tatyana; Schmid, Ralf; Davies, Noel W; Storey, Nina M; Dorlet, Pierre; Moody, Peter C E; Mitcheson, John S; Raven, Emma L

CRISPR/Cas9 directed to the Ube3a antisense transcript improves Angelman syndrome phenotype in mice

利用 CRISPR/Cas9 技术靶向 Ube3a 反义转录本可改善小鼠的安格曼综合征表型。

Schmid, Ralf S; Deng, Xuefeng; Panikker, Priyalakshmi; Msackyi, Msema; Breton, Camilo; Wilson, James M

Correction to: Chd8 haploinsufficiency impairs early brain development and protein homeostasis later in life

更正:Chd8 单倍体不足会损害早期大脑发育和晚年蛋白质稳态

Jiménez, Jessica A; Ptacek, Travis S; Tuttle, Alex H; Schmid, Ralf S; Moy, Sheryl S; Simon, Jeremy M; Zylka, Mark J

Discovery of a heme-binding domain in a neuronal voltage-gated potassium channel

在神经元电压门控钾通道中发现血红素结合域

Burton, Mark J; Cresser-Brown, Joel; Thomas, Morgan; Portolano, Nicola; Basran, Jaswir; Freeman, Samuel L; Kwon, Hanna; Bottrill, Andrew R; Llansola-Portoles, Manuel J; Pascal, Andrew A; Jukes-Jones, Rebekah; Chernova, Tatyana; Schmid, Ralf; Davies, Noel W; Storey, Nina M; Dorlet, Pierre; Moody, Peter C E; Mitcheson, John S; Raven, Emma L

Lipid⁻Protein Interactions in Niemann⁻Pick Type C Disease: Insights from Molecular Modeling

尼曼-匹克C型疾病中的脂质-蛋白质相互作用:来自分子建模的启示

Wheeler, Simon; Schmid, Ralf; Sillence, Dan J

A mechanism for CO regulation of ion channels

一氧化碳调节离子通道的机制

Kapetanaki, Sofia M; Burton, Mark J; Basran, Jaswir; Uragami, Chiasa; Moody, Peter C E; Mitcheson, John S; Schmid, Ralf; Davies, Noel W; Dorlet, Pierre; Vos, Marten H; Storey, Nina M; Raven, Emma